Transfusion Medicine
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- 2002
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Mark
Molecular basis of the globoside-deficient P(k) blood group phenotype. Identification of four inactivating mutations in the UDP-N-acetylgalactosamine: globotriaosylceramide 3-beta-N-acetylgalactosaminyltransferase gene.
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- Contribution to journal › Article
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Mark
Novel alleles at the JK blood group locus explain the absence of the erythrocyte urea transporter in European families.
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- Contribution to journal › Article
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Mark
Phenotype prediction by DNA-based typing of clinically significant blood group systems in Jordanian blood donors.
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- Contribution to journal › Article
- 2001
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Mark
Intercellular adhesion molecule-4 binds alpha(4)beta(1) and alpha(V)-family integrins through novel integrin-binding mechanisms
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- Contribution to journal › Article
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Mark
Genomic analysis of clinical samples with serologic ABO blood grouping discrepancies: identification of 15 novel A and B subgroup alleles
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- Contribution to journal › Article
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Mark
The ABO blood group gene: a locus of considerable genetic diversity
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- Contribution to journal › Article
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Mark
Polymorphism and recombination events at the ABO locus: a major challenge for genomic ABO blood grouping strategies
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- Contribution to journal › Article
- 2000
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Mark
Genomic characterization of the kidd blood group gene:different molecular basis of the Jk(a-b-) phenotype in Polynesians and Finns
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- Contribution to journal › Article
- 1999
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Mark
Allele-related variation in minisatellite repeats involved in the transcription of the blood group ABO gene
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- Contribution to journal › Article
- 1998
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Mark
The Fy(x) phenotype is associated with a missense mutation in the Fy(b) allele predicting Arg89Cys in the Duffy glycoprotein
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- Contribution to journal › Article